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3,6-Anhydro-L-galactose increases hyaluronic acid production via the EGFR and AMPK alpha signaling pathway in HaCaT keratinocytes

Authors
Lee, Jae-EunKim, Young-AhYu, SoraPark, So YoungKim, Kyoung HeonKang, Nam Joo
Issue Date
Dec-2019
Publisher
ELSEVIER IRELAND LTD
Keywords
3,6-Anhydro-L-galactose; Skin hydration; Hyaluronic acid; Hyaluronan synthase 2; Epidermal growth factor receptor; Keratinocyte
Citation
JOURNAL OF DERMATOLOGICAL SCIENCE, v.96, no.2, pp.90 - 98
Indexed
SCIE
SCOPUS
Journal Title
JOURNAL OF DERMATOLOGICAL SCIENCE
Volume
96
Number
2
Start Page
90
End Page
98
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/61481
DOI
10.1016/j.jdermsci.2019.10.005
ISSN
0923-1811
Abstract
Background: Hyaluronic acid (HA) is an important factor in skin hydration maintenance. In mammalian keratinocytes, hyaluronan synthase 2 (HAS2) is a critical enzyme in HA production. Therefore, the promotion of HAS2 expression in keratinocytes may be a strategy for maintaining skin moisture. Objective: The aim was to determine the skin hydration effect and regulatory mechanisms of 3,6-anhydro-L-galactose (L-AHG), a main component of red macroalgal carbohydrates in human keratinocytes. Methods: L-AHG was applied to an immortalized human epidermal keratinocyte cell line (HaCaT cells). HA production, HAS2 protein and mRNA levels, and the activation of the signaling pathways involved in HAS2 expression were measured. HA levels were also evaluated for three dimensional (3D) reconstructed human skin. Results: Our results suggest that L-AHG upregulates HA production and may enhance HAS2 expression by activating EGFR-mediated ERK, PI3K/Akt, and STAT3 signaling pathways. We confirmed that L-AHG activated the AMPK signaling pathway which in turn could regulate HAS2 expression in HaCaT cells. The effects of L-AHG on HA production were observed in the 3D reconstructed human skin model. Conclusion: Our results suggest that L-AHG may enhance skin moisture retention by increasing HA synthesis in human epidermal keratinocytes. (C) 2019 The Author(s). Published by Elsevier B.V. on behalf of Japanese Society for Investigative Dermatology.
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